Sulphate, Nitrogen and Base Cation Budgets at 21 Forested Catchments in Canada, the United States and Europe

To assess the concern over declining base cation levels in forest soils caused by acid deposition, input-output budgets (1990s average) for sulphate (SO₄), inorganic nitrogen (NO₃-N; NH₄-N), calcium (Ca), magnesium (Mg) and potassium (K) were synthesised for 21 forested catchments from 17 regions in Canada, the United States and Europe. Trend analysis was conducted on monthly ion concentrations in deposition and runoff when more than 9 years of data were available (14 regions, 17 sites). Annual average SO₄ deposition during the 1990s ranged between 7.3 and 28.4 kg ha⁻¹ per year, and inorganic nitrogen (N) deposition was between 2.8 and 13.8 kg ha⁻¹ per year, of which 41–67% was nitrate (NO₃-N). Over the period of record, SO₄ concentration in deposition decreased in 13/14 (13 out of 14 total) regions and SO₄ in runoff decreased at 14/17 catchments. In contrast, NO₃-N concentrations in deposition decreased in only 1/14 regions, while NH₄-N concentration patterns varied; increasing at 3/14 regions and decreasing at 2/14 regions. Nitrate concentrations in runoff decreased at 4/17 catchments and increased at only 1 site, whereas runoff levels of NH₄-N increased at 5/17 catchments. Decreasing trends in deposition were also recorded for Ca, Mg, and K at many of the catchments and on an equivalent basis, accounted for up to 131% (median 22%) of the decrease in acid anion deposition. Base cation concentrations in streams generally declined over time, with significant decreases in Ca, Mg and K occurring at 8, 9 and 7 of 17 sites respectively, which accounted for up to 133% (median 48%) of the decrease in acid anion concentration. Sulphate export exceeded input at 18/21 catchments, likely due to dry deposition and/or internal sources. The majority of N in deposition (31–100%; median 94%) was retained in the catchments, although there was a tendency for greater NO₃-N leaching at sites receiving higher (<7 kg ha^-1 per year) bulk inorganic N deposition. Mass balance calculations show that export of Ca and Mg in runoff exceeds input at all 21 catchments, but K export only exceeds input at 16/21 sites. Estimates of base cation weathering were available for 18 sites. When included in the mass balance calculation, Ca, Mg and K exports exceeded inputs at 14, 10 and 2 sites respectively. Annual Ca and Mg losses represent appreciable proportions of the current exchangeable soil Ca and Mg pools, although losses at some of the sites likely occur from weathering reactions beneath the rooting zone and there is considerable uncertainty associated with mineral weathering estimates. Critical loads for sulphur (S) and N, using a critical base cation to aluminium ratio of 10 in soil solution, are currently exceeded at 7 of the 18 sites with base cation weathering estimates. Despite reductions in SO₄ and H⁺ deposition, mass balance estimates indicate that acid deposition continues to acidify soils in many regions with losses of Ca and Mg of primary concern. The U.S. Government's right to retain a non-exclusive, royalty free licence in and to any copyright is acknowledged. The Canadian Crown reserves the right to retain a non-exclusive, royalty free licence in and to any copyright.     

Acidification at Plastic Lake,Ontario: Has 20 Years Made a Difference?

In response to reduced sulphur emissions, there has been a large decrease in sulphate (; −0.97 μeq l⁻¹ year⁻¹) and hydrogen (−1.18 μeq l⁻¹ year⁻¹) ion concentration in bulk precipitation between 1980 and 2000 at Plastic Lake in central Ontario. The benefit of this large reduction in deposition on stream water chemistry was assessed using the gauged outflow from a conifer-forested catchment (PC1; 23.3 ha), which is influenced by a small wetland located immediately upstream of the outflow. Sulphate concentrations declined, but not significantly due to large inter-annual variation in concentration. Between 1980 and 2000, there were significant increases in dissolved organic carbon, ammonium and potassium concentration likely reflecting increased mineralisation in the wetland. Calcium concentrations in PC1 decreased during the two decade period (−2.24 μeq l⁻¹ year⁻¹), as a consequence there was no improvement in stream pH and the Ca:Al ratio in PC1 continued to decline. A similar response was noted in an upland-draining sub-catchment of PC1-08 that has been monitored since 1987. Despite large reductions in deposition and almost complete retention of nitrogen in soil, there has been no improvement (in terms of pH) in stream water at PC1 due to a combination of soil acidification and climatic (droughts, increased mineralisation) perturbations.     

Trail following in ants: individual properties determine population behaviour

This paper deals with the purposeful marking of trails as a mechanism for coordinating movement. Patterns of motion are adapted to the environmental conditions, the functions to be carried out, and the condition of the organism; therefore, the networks of trails must change both quantitatively and qualitatively over time. The nature of such changes, and how they are controlled at the individual level are discussed. In particular, we show that slight modulations in individual traits, in the trail marker, or in the size of the group can account for major changes in movement patterns at the population level such as abrupt transitions from diffuse area-covering networks to focused trunk trails. Using a mathematical model and computer (cellular automata) simulation we show that trunk trails carrying a high density of traffic can form spontaneously under suitable conditions from an initially randomly distributed group. The key to this self-organizing property stems from interactions between individuals that lead to a collective effect in recruitment to trails: the influence of small groups of individuals increases rapidly with group size. The dichotomy between high traffic (strong) trunk trails versus diffuse (weak) networks is discussed.     

Drought-induced sulphate release from a wetland in south-central Ontario

Increased sulphate (SO₄) export from wetlands following summer droughts in central Ontario, Canada has been associated with the delayed chemical recovery of downstream surface waters following decreased sulphur (S) emissions. Prolonged summer droughts result in a decrease or cessation of stream flow, declines in wetland water table level and oxidation of reduced S compounds to SO₄, which is subsequently flushed into drainage streams when stream flow resumes. Sulphate input-output budget calculations (1983–1995 and 1999–2001) at a conifer Sphagnum swamp in the Plastic Lake catchment, indicate that SO₄ is retained in most years but is exported on a net basis following particularly severe summer droughts that result in the cessation of stream flow for more than 54 days (95% CI: 41–72 days). Hindcast calculations using long-term (1916–2000) stream discharge records from a nearby station indicate that while droughts occurred frequently in south-central Ontario over the past 85 years, sufficiently dry conditions to cause net SO₄ export occurred in only18 of the past 85 years, and indicate a cumulative positive SO₄ balance for the swamp (i.e. net SO₄ retention). Furthermore, the S pool at the Plastic Lake swamp has been estimated to be ∼1500 kg S/ha in the upper 40 cm peat layer, which is large compared to the amount of net SO₄ export that occurs even in years with particularly dry summers (e.g. −43 kg S/ha in 1987/88). Together, these data suggest that the wetland S pool at Plastic Lake has not been depleted by previous droughts and will continue to sustain episodic drought-related SO₄ export for the foreseeable future.     

Dispersal and mobility of heavy metals in relation to tree survival in an aerially contaminated woodland soil

Nearly a century of metal deposition adjacent to a metal refinery in Prescot, north-west England has led to highly elevated metal levels in soils at a dominantly Acer pseudoplatanus woodland, but with incongruously and perplexingly few detrimental effects on trees. Dispersal and speciation of Cu, Cd, Zn, Pb and Ni in soil was found to be extremely variable, but spatial patterns of metals were inter-related and also related to soil pH and soil organic matter. These soil variables were all generally higher in soil directly beneath trees than in soil between trees, and were particularly high beneath the spreading canopy of Aesculus hippocastanum. It is argued that this heterogeneous dispersal and availability of metals in soils may explain the survival of mature trees and the successful establishment of seedlings within the woodland. Differing speciation and mobility has allowed high disappearance rates of metals since recent closure of the refinery, which may result in soil recovery at a faster rate than previously thought.     

An assessment of the nutrient status of sugar maple in Ontario: indications of phosphorus limitation

Soil acidification, caused by elevated anthropogenic deposition, has led to concerns over nutrient imbalances in Ontario's sugar maple (Acer saccharum Marsh.) forests. In this study, soil chemistry, foliar chemistry, crown condition, and tree growth were measured at 36 sugar maple stands that included acidic (pH?相似文献   

Monitoring historical changes in soil and atmospheric trace metal levels by dendrochemical analysis

The use of dendrochemistry for monitoring historical changes in trace metal deposition and mobilisation of metals in soils is evaluated. In experimental studies, mobilisation of trace metals in surface soil following deliberate acidification was recorded in sugar maple (Acer saccharum) tree-rings with minimal lateral movement between rings. Furthermore, positive correlations between wood (3 year section 1993-95) and foliar chemistry (mean concentration 1993-95) were found for Cd and Zn, but not for Cu and Ni, showing that mobility up the tree bole differs between metals. Even so, substantial lateral movement of elements between rings occurs in some species. Stable Pb isotope ratios in tree-rings were used to show that sacred fir (Abies religeosa) is not a useful monitor of Pb deposition because Pb accumulates in the heartwood. Numerous sophisticated analytical techniques are now used in dendrochemical studies, including laser ablation sampling in conjunction with inductively coupled plasma mass spectrometry that enable the multi-element analysis of extremely small tree-rings with low detection limits. Clearly, not all tree species are suitable for dendrochemical studies, but if careful sampling strategies are used and suitable tree species are chosen, the chemical analysis of tree-rings can provide information concerning historical changes in soil and atmospheric trace metal levels unavailable from any other source.     

Soil acidification and foliar nutrient status of Ontario's deciduous forest in 1986 and 2005

To assess the impacts of the decline in sulphur (S) deposition over the past 20 years in Ontario, soil chemistry and sugar maple (Acer saccharum Marsh) foliar chemistry were measured at 17 sites in south and central Ontario in 2005 and compared with archived samples collected in 1986. Foliar S concentrations were lower in 2005, reflecting the decline in S deposition whereas foliar N remained unchanged, reflecting the lack of change in N deposition in Ontario. Mineral soil pH, exchangeable base cations were lower in 2005 whereas total S, N and cation exchange capacity (CEC) were unchanged. Foliar concentrations of Ca were positively related to soil Ca levels in the A-horizon and were lower in 2005. Despite evidence of increasing soil acidity and losses of calcium, foliar base cation concentrations at most sites were adequate for sugar maple and forest health in terms of canopy appearance (Decline Index) improved.     

The quantification and distribution of pollution Pb at a woodland in rural south central Ontario, Canada

Lead concentrations and Pb isotope ratios were measured in the forest floor, mineral soil and vegetation at a white pine and a sugar maple stand in a woodland in south central Ontario. Lead concentrations decreased and 206Pb/207Pb ratios increased with mineral soil depth reflecting the mixing of pollution and natural Pb sources. Lead concentrations and 206Pb/207Pb ratios at 20-30 cm depth were approximately 6-7 mg/kg and 1.31-1.32, respectively. Assuming an integrated 206Pb/207Pb ratio in deposition over time of 1.18, estimated from lichen measurements and published data for the region, approximately 65% of Pb in the surface (0-1 cm) mineral soil is from anthropogenic sources. Approximately 90% of pollution Pb is found in the 0-10 cm soil layer (Ah) and less than 3% of the pollution Pb is present in the forest biomass and mull-type forest floor combined. Despite low Pb concentrations in vegetation (<2.5 mg/kg), we estimate that between 65 and 100% of the Pb in vegetation and approximately 75% of the Pb in the forest floor is from pollution sources. In total, the pollution Pb burdens at the pine and maple stands are estimated to be 860 and 750 mg/m2, respectively.     

Analysis of tree rings using inductively coupled plasma mass spectrometry to record fluctuations in a metal pollution episode

Analysis of Acer pseudoplatanus L. (sycamore) tree rings using ICP-MS was used to assess the impact of metal deposition on trees growing in the vicinity of a metal refinery at Prescot, north-west England compared to a reference site at Croxteth 6 km distant receiving minimal deposition. No difference in tree growth between sites was recorded. Large reductions in Cu and Cd deposition since the late 1970s was accompanied by a steep decline in Cd concentrations in the outer rings in trees close to the refinery. A similar reduction in Cu concentrations was less apparent due to a tendency for Cu to increase in the outer rings. Zinc and Ni were higher in xylem at Prescot compared to Croxteth. There was no trend in Zn concentrations at either site although Ni concentrations increased in trees close to the refinery after 1982. Manganese concentrations in xylem were much higher at Prescot; Mn levels declined until the late 1970s and then increased slightly in later years interspersed by large concentration peaks within individual years during the 1980s. There was little change in Mn concentrations in trees at Croxteth during this period. Calcium, Mg and Sr concentrations remained steady or declined slightly in rings formed since 1965 in trees at Croxteth. Concentrations of Ca, Mg and Sr were higher in rings formed prior to the mid 1970s in trees at Prescot, but declined steadily after this period, although peaks in concentrations of each element were recorded in individual years during the 1980s. Phosphorous concentrations in rings increased towards the cambium at Croxteth, although P levels decreased in rings formed after 1982 at Prescot. No difference in K concentrations between sites was recorded. Lead concentrations in xylem at both sites declined steadily in rings formed after 1970, although concentrations were higher at the reference site. Analysis of individual sycamore tree rings appears to record short-term changes in pollution episodes, with little lateral movement of elements occurring. It is suggested that changes in element concentrations in trees close to the refinery are a result of reduced metal deposition combined with increased soil acidity due to reduced buffering capacity of metal ions in rainfall.